Canonical Allele Identifier: CA2636791112
Gene: NOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27804105A>G , CM000679.2:g.27804105A>G GRCh38
NC_000017.10:g.26131131A>G , CM000679.1:g.26131131A>G GRCh37
NC_000017.9:g.23155258A>G NCBI36
NG_011470.1:g.1425T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000582441.1:c.438+18T>C ENSP00000462879.1:n.438+18T>C
XM_011524859.1:c.-74+18T>C XP_011523161.1:n.-74+18T>C